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Clean method for preparing layered double hydroxides

a technology of layered double hydroxide and layered hydroxide, which is applied in the field of clean method for preparing layered double hydroxide, can solve the problems of increasing solubility, difficult to dissolve in water, and low product constant of hydrogen oxide, so as to avoid the use reduce the effect of atom efficiency and avoid the effect of naoh or other materials

Active Publication Date: 2008-07-17
BEIJING UNIV OF CHEM TECH
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

[0011]Only M2+(OH)2, M3+(OH)3, and CO2 or HnAn− are used in this method. Use of NaOH or other materials has been avoided. All the atoms of the reactants are incorporated into the target product. Therefore the atom efficiency of this reaction is 100% which is a typical atom-economical reaction. In addition, the process of washing and filtration can be omitted because there is no by-product, such that the environment can be protected and water resource is also saved.
[0020]The present invention is advantageous in that all the atoms of reactants are converted into the target product and there is no by-product; the pure product can be obtained by drying the target product without washing so that a large amount of water can be saved with considerable benefit to the environment.

Problems solved by technology

Most metal hydroxides have low solubility product constants and are difficult to dissolve in water.
Their solubility increases at high temperatures and pressures.

Method used

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  • Clean method for preparing layered double hydroxides
  • Clean method for preparing layered double hydroxides
  • Clean method for preparing layered double hydroxides

Examples

Experimental program
Comparison scheme
Effect test

example 1

[0024]MgAl—CO3-LDHs were prepared as follows.

[0025]Step A: Total 10 g Mg(OH)2 and Al(OH)3 with a molar ratio of Mg2+ / Al3+=2:1 were put into 90 g of deionized water, and the resulting mixture was transferred to a three-necked flask fitted with a reflux device.

[0026]Step B: The mixture was heated to 100° C. under stirring for four days, while CO2 was fed thereto at a flow rate of 10 ml / min. The resulting slurry product was filtered and dried in air at 70° C. for 8 h to give Mg4Al2(OH)12CO3.4H2O.

[0027]The powder XRD patterns of the prepared Mg4Al2(OH)12CO3.4H2O were recorded using a Shimadzu XRD-6000 diffractometer, and were shown in FIG. 1. The typical peaks which correspond to the (003), (006), (009) reflections were found at 2θ=11.7°, 23.4°, 34.5°. It could be concluded from the patterns that the samples had a layered crystal structure.

[0028]The infrared spectra of the samples, obtained using a Bruker Vector 22 model Fourier transform infrared spectrometer (FT-IR), were shown in FIG...

example 2

[0029]Ni8Fe2(OH)20(C8H4O4).4H2O was prepared as follows.

[0030]Step A: Total 5 g Ni(OH)2 and Fe(OH)3 with a molar ratio of Ni2+ / Fe3+=4:1 were put into 90 g of deionized water, and the resulting mixture was transferred to a three-necked flask fitted with a reflux device.

[0031]Step B: 0.58 g terephthalic acid was added to the flask. The contents in the flask were heated to 100° C. and reacted for eight days under stirring. After filtration and drying in air at 70° C. for 8 h, Ni8Fe2(OH)20(C8H4O4).4H2O was obtained.

[0032]The TEM image of the product produced in example 2, obtained using a Hitachi S-3500N scanning electron microscope, was shown in FIG. 3. The image reveals a layered hexagonal morphology of LDHs.

example 3

[0033]ZnMg3Al2(OH)12CO3.4H2O was prepared as follows.

[0034]Step A: Total 20 g Zn(OH)2, Mg(OH)2 and Al(OH)3 with a molar ratio of Zn2+ / Mg3+ / Al3+=1:3:2 were put into 80 g of deionized water, and the mixture was transferred to an airtight reactor fitted with a churn-dasher.

[0035]Step B: After adding 40 g of dry ice to the reactor, the system was heated at 150° C. for one day under stirring. The resulting slurry was filtered and dried in air at 70° C. for 8 h to give ZnMg3Al2(OH)12CO3.4H2O.

[0036]Elemental analysis of the product obtained in example 3 was performed on an ICPS-7500 inductively coupled plasma spectrometer. The molar ratio of Zn:Mg:Al was measured as 1:3:2 and no Na+ was found in the product.

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Abstract

Disclosed is a clean method for preparing layered double hydroxides (LDHs), in which hydroxides of different metals are used as starting materials for production of LDHs by atom-economical reactions. The atom efficiency of the reaction is 100% in each case because all the atoms of the reactants are converted into the target product since only M2+(OH)2, M3+(OH)3, and CO2 or HnAn− are used, without any NaOH or other materials. Since there is no by-product, filtration or washing process is unnecessary. The consequent reduction in water consumption is also beneficial to the environment.

Description

CROSS-REFERENCE TO RELATED APPLICATIONS[0001]The present patent application claims priority from Chinese Patent Application No. 200710062650.9, filed on Jan. 12, 2007.TECHNICAL FIELD[0002]The present invention relates to a clean method for preparing layered double hydroxides, and belongs to the field of synthesis of inorganic nonmetallic functional materials.TECHNICAL BACKGROUND[0003]Layered double hydroxides (LDHs), which belong to a typical family of anionic layered materials, can be represented by the general formula [M2+1-xM3+x(OH)2]x+(An−)x / n.mH2O, where M2+ is a bivalent metal cation, M3+ is a trivalent metal cation, An− denotes an interlayer anions with negative charge n, m is the number of interlayer water molecules, and x is the molar ratio of the M3+ to the sum of the M3+ and M2+. The identity and ratio of the layer elements as well as the interlayer guest anions can be adjusted over a wide range in order to obtain materials with specific structures and properties. Because...

Claims

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Application Information

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IPC IPC(8): C01B31/00C01B25/12C07F15/02
CPCC01F7/004C07F15/045C01G9/02C01G45/00C01G45/02C01G49/00C01G49/02C01G51/00C01G51/02C01P2002/22C01P2002/72C01P2002/74C01P2002/82C01P2004/04C01P2004/20C01G9/00C01G53/006C01G9/006C01G49/009C01F7/784C01F7/785
Inventor DUAN, XUELI, DIANQINGLV, ZHILIN, YANJUNXU, XIANGYU
Owner BEIJING UNIV OF CHEM TECH
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